Najim Ameziane

Rostock, MV, Germany

Last Updated: 09/26/2026

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Found 42 publications

Insight into Haploinsufficiency of the ERBB4 Gene: Expanding the Spectrum of Associated Phenotypes.

Insight into Haploinsufficiency of the ERBB4 Gene: Expanding the Spectrum of Associated Phenotypes.

Journal: Journal of autism and developmental disorders

Published: March 21, 2025

A deep intronic mutation causes RAD50 deficiency through an unusual mechanism of distant exon activation.

A deep intronic mutation causes RAD50 deficiency through an unusual mechanism of distant exon activation.

Journal: The Journal of clinical investigation

Published: December 12, 2024

Loss of tissue-type plasminogen activator causes multiple developmental anomalies.

Loss of tissue-type plasminogen activator causes multiple developmental anomalies.

Journal: Brain communications

Published: June 20, 2024

Relevance of genetic testing in the gene-targeted trial era: the Rostock Parkinson's disease study.

Relevance of genetic testing in the gene-targeted trial era: the Rostock Parkinson's disease study.

Journal: Brain : a journal of neurology

Published: December 12, 2023

Microbial contamination and composition of oral samples subjected to clinical whole genome sequencing.

Microbial contamination and composition of oral samples subjected to clinical whole genome sequencing.

Journal: Frontiers in genetics

Published: October 27, 2022

Clonal and "Intrinsic" Heterogeneity of Somatic Variants in Microsatellite-Stable Colorectal Carcinomas and Their Metastases.

Clonal and "Intrinsic" Heterogeneity of Somatic Variants in Microsatellite-Stable Colorectal Carcinomas and Their Metastases.

Journal: Laboratory investigation; a journal of technical methods and pathology

Published: October 19, 2022

Secondary findings in a large Pakistani cohort tested with whole genome sequencing.

Secondary findings in a large Pakistani cohort tested with whole genome sequencing.

Journal: Life science alliance

Published: August 16, 2022

Publisher Correction: BIRC2-BIRC3 amplification: a potentially druggable feature of a subset of head and neck cancers in patients with Fanconi anemia.

Publisher Correction: BIRC2-BIRC3 amplification: a potentially druggable feature of a subset of head and neck cancers in patients with Fanconi anemia.

Journal: Scientific reports

Published: April 07, 2022

The Inhibitory Response to PI3K/AKT Pathway Inhibitors MK-2206 and Buparlisib Is Related to Genetic Differences in Pancreatic Ductal Adenocarcinoma Cell Lines.

The Inhibitory Response to PI3K/AKT Pathway Inhibitors MK-2206 and Buparlisib Is Related to Genetic Differences in Pancreatic Ductal Adenocarcinoma Cell Lines.

Journal: International journal of molecular sciences

Published: March 21, 2022

Inhibitory Response to CK II Inhibitor Silmitasertib and CDKs Inhibitor Dinaciclib Is Related to Genetic Differences in Pancreatic Ductal Adenocarcinoma Cell Lines.

Inhibitory Response to CK II Inhibitor Silmitasertib and CDKs Inhibitor Dinaciclib Is Related to Genetic Differences in Pancreatic Ductal Adenocarcinoma Cell Lines.

Journal: International journal of molecular sciences

Published: March 18, 2022

Immune dysregulation caused by homozygous mutations in CBLB.

Immune dysregulation caused by homozygous mutations in CBLB.

Journal: The Journal of clinical investigation

Published: August 27, 2021

A disorder clinically resembling cystic fibrosis caused by biallelic variants in the AGR2 gene.

A disorder clinically resembling cystic fibrosis caused by biallelic variants in the AGR2 gene.

Journal: Journal of medical genetics

Published: August 11, 2021

Showing 1-12 of 42

Last Updated: 09/26/2026